Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_provenance.
- NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_assertion description "[The Finnish type of familial amyloid polyneuropathy (FAF) is an autosomal dominant form of systemic amyloidosis caused by a mutation in the gelsolin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_provenance.
- NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_assertion evidence source_evidence_literature NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_provenance.
- NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_assertion SIO_000772 1322359 NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_provenance.
- NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_assertion wasDerivedFrom befree-2016 NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_provenance.
- NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_assertion wasGeneratedBy ECO_0000203 NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_provenance.
- befree-2016 importedOn "2016-02-19" NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_provenance.